A newborn girl with seizures and persistent hypoglycemia

New England Journal of Medicine

Volumn 345, Issue 25, 2001, Pages 1833-1839

  Sadeghi Nejad, A ^a   Graeme Cook, F M ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

GLUCOSE; INSULIN;

ARTICLE; BLOOD CHEMISTRY; CASE REPORT; CLINICAL FEATURE; DIFFERENTIAL DIAGNOSIS; FEMALE; HUMAN; HUMAN TISSUE; HYPERINSULINISM; HYPOGLYCEMIA; IMMUNOHISTOCHEMISTRY; INSULINOMA; NEWBORN; NUCLEAR MAGNETIC RESONANCE IMAGING; PANCREAS EXOCRINE INSUFFICIENCY; PANCREAS ISLET CELL HYPERPLASIA; PANCREAS RESECTION; PRIORITY JOURNAL; TOTAL PARENTERAL NUTRITION; HYPERPLASIA; PANCREAS; PANCREAS DISEASE; PANCREAS ISLET; PATHOLOGY; SEIZURE;

CASE REPORT; DIAGNOSIS, DIFFERENTIAL; FEMALE; GLUCOSE; HUMAN; HYPERINSULINISM; HYPERPLASIA; HYPOGLYCEMIA; INFANT, NEWBORN; ISLETS OF LANGERHANS; PANCREAS; PANCREATIC DISEASES; PARENTERAL NUTRITION, TOTAL; SEIZURES;

EID: 0035924265     PISSN: 00284793     EISSN: None     Source Type: Journal    
DOI: 10.1056/NEJMcpc392001     Document Type: Article

References (25)

1. Hypoglycemia: A pathophysiologic approach
2. The causes of neonatal hypoglycemia
3. Circulation and energy metabolism of the brain
4. Human fetal insulin response to sustained maternal hyperglycemia
5. Maturation of insulin response to glucose during human fetal and neonatal development: Studies with perifusion of pancreatic isletlike cell clusters
6. Clinical features of 52 neonates with hyperinsulinism
7. Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene
8. An autosomal dominant form of familial persistent hyperinsulinemic hypoglycemia of infancy, not linked to the sulfonylurea receptor locus
9. Familial hyperinsulinism with apparent autosomal dominant inheritance: Clinical and genetic differences from the autosomal recessive variant
10. Recent advances in hyperinsulinism and the pathogenesis of diabetes mellitus
11. Persistent neonatal hyperinsulinism
12. Familial hyperinsulinism maps to chromosome 11p14-15.1, 30 cM centromeric to the insulin gene
13. Genetic heterogeneity in familial hyperinsulinism
14. Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy
15. A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinism
16. Familial and sporadic hyperinsulinism: Histopathologic findings and segregation analysis support a single autosomal recessive disorder
17. Mosaic uniparental disomy in Beckwith-Wiedemann syndrome
18. Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomy
19. Paternal mutation of the sulfonylurea receptor (SURI) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia
20. Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor gene
21. Persistent hyperinsulinemic hypoglycemia of infancy: Long-term octreotide treatment without pancreatectomy
22. Ionic control of beta cell function in nesidioblastosis: A possible therapeutic role for calcium channel blockade
23. Value of selective pancreatic angiography in the evaluation of hyperinsulinemic hypoglycemia in infancy
24. Hyperinsulinism in children: Diagnostic value of pancreatic venous sampling correlated with clinical, pathological and surgical outcome in 25 cases
25. Dual phase spiral CT in the detection of small insulinomas of the pancreas